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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1969183Generated: October 30, 2026

Dimethylformamide → 3-Bromo-5-(tert-butyl-dimethyl-silanyloxy)-benzaldehyde

https://huagongshe.com/reaction/1969183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantAmmonium ChlorideHCID 25517—
ReactantTert-butyl(3,5-dibromophenoxy)dimethylsilaneHCID 21762106—
ReactantButyllithiumHCID 178418339—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product3-Bromo-5-(tert-butyl-dimethyl-silanyloxy)-benzaldehydeHCID 57791901—

Reaction Conditions

Temperature-78 °C

Reaction Steps

tert-Butyl-(3,5-dibromo-phenoxy)-dimethyl-silane (22 g; 60.08 mmol) was dissolved in THF (200 mL) in a dried reaction flask under an atmosphere of nitrogen. The mixture was cooled to −78° C. and n-BuLi (1.6 N in hexane; 41.25 mL; 66.09 mmol) was added while the temperature was kept between −60 and −78° C. The mixture was stirred for 15 min. and DMF (4.83 g; 66.08 mmol) was added. The reaction mixture was stirred for 1 h and methanol (5 mL) followed by saturated ammonium chloride was added. Ethyl acetate (200 mL) was added and the organic phase was separated from the aqueous phase. The organic phase was washed with water, dried, and evaporated to dryness. The crude product was purified by flash chromatography (heptane:dichloromethane (1:1). Yield 7 g. HPLC-MS: m/z: 317.0 (M+1); Rt: 2.7 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426473B2
Source datasetuspto-grants-2013_04
ORD IDord-bd426ee76bda4d2d9673dc00c3dcc21b
Source noteuspto-grants-2013_04